chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	80783493	80783494	T	C	33	GENIC	homozygous	109875592
2	80783937	80783938	C	T	21	GENIC	homozygous	110714117
2	80784212	80784213	C	A	19	GENIC	homozygous	110714118
2	80785190	80785191	T	C	27	GENIC	homozygous	110714119
2	80785401	80785402	A	C	23	GENIC	homozygous	109875600
2	80785523	80785524	A	G	22	GENIC	homozygous	110714120
2	80786231	80786232	T	C	13	GENIC	homozygous	110714121
2	80786802	80786803	T	C	34	GENIC	homozygous	109875608
2	80786936	80786937	C	A	27	GENIC	homozygous	110714123
2	80787784	80787785	T	C	18	GENIC	homozygous	109875610
2	80787989	80787990	G	C	32	GENIC	homozygous	109875612
2	80788288	80788289	T	C	18	GENIC	homozygous	109875614
2	80788311	80788312	T	C	19	GENIC	homozygous	109875616
2	80788420	80788421	A	T	44	GENIC	homozygous	109875618
2	80788627	80788628	G	A	38	GENIC	homozygous	110714124
2	80789060	80789061	T	C	39	GENIC	homozygous	110714125
2	80789095	80789096	T	C	31	GENIC	homozygous	110714126
2	80789424	80789425	C	T	24	GENIC	homozygous	110714127
2	80789458	80789459	C	G	25	GENIC	homozygous	110714128
2	80789650	80789651	C	A	8	GENIC	homozygous	110714129
2	80790124	80790125	G	A	21	GENIC	homozygous	110714130
2	80791923	80791924	C	T	32	GENIC	homozygous	110714131
2	80792239	80792240	T	G	28	GENIC	homozygous	109875624
2	80792383	80792384	C	T	22	GENIC	homozygous	110714132